exam 2 ch 13 Flashcards

1
Q

The branch of evolutionary biology that studies the diversity of reproductive
strategies

A

life-history analysis

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2
Q

Have a high growth rate but low survivability (“cheap” offspring)

A

r-selected species

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3
Q

Have a low growth rate but high survivability (“expensive” offspring)

A

K-selected species

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4
Q

Changes in life history are caused by changes in the?

A

allocation of energy

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5
Q

Number of gametes produced by an individual

A

Fecundity

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6
Q

selection will favor the number of offspring that results in the most surviving
offspring

A

Lack’s Hypothesis

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7
Q

individual offspring survival decreases with increasing offspring number

A

Trade-off

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8
Q

Energy contained in the offspring themselves

A

Direct costs

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9
Q

Energy expended to produce and carry them

A

indirect costs

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10
Q
  1. (a) There is a trade-off between size and number of offspring.
  2. (b) Above a minimum size, the probability that any individual offspring will survive is an increasing
    function of its size
A

Selection on Offspring Size
Assumptions

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11
Q

selection on Offspring Size

A

-Selection on parents favors a compromise
between the quality and quantity of offspring,
-Selection on individual offspring favors
high quality

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12
Q

Fertilization of two or more ova from the same cycle by sperm from separate
acts of sexual intercourse

A

Superfecundation

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13
Q

Only one copy of a gene in an individual (from mother or father) is expressed,
while the other copy is suppressed

A

Genomic imprinting

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14
Q

A growth promoting hormone.

A

Insulin-like growth factor II

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15
Q

A receptor that binds IGF-II to promote
lysosome activity

A

Cation-independent mannose-6-phosphate receptor (CI-MPR)

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16
Q

When mates are not monogamous, the life-history strategy that is ___________________________ for the other

A

optimal for one sex may be
suboptimal

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17
Q

Life-history traits have ________________________ than other traits.

A

lower heritabilities

18
Q

Low heritability means traits are more influenced by?

A

environmental factors

19
Q

Higher reproductive capacity allowed dinosaurs to?

A

recover more quickly from population bottlenecks

20
Q

Describes the molecular changes seen in most aging cells

A

The Hallmarks of Aging

21
Q

There are 2 main models of aging;

A
  1. Damaged-based model
  2. Programmatic models
22
Q
  1. Damaged-based model
A

(Damage to DNA and cells accumulates)

23
Q
  1. Programmatic models
A

(Aging is encoded in the DNA)

24
Q

Mammals with higher somatic mutation rates have ______ lifespans

A

shorter

25
Q

non-sex cells

A

somatic cells

26
Q

are highly reactive chemicals formed from diatomic oxygen (O2),
water, and hydrogen peroxide. Some prominent ROS are hydroperoxide (-OOH), superoxide (O2-),
hydroxyl radical (OH.)

A

Reactive oxygen species (ROS)

27
Q

During DNA replication, at the end of the lagging the final RNA primer is
removed leaving a small site that is not replicated by polymerase, meaning that there will be a small
amount of DNA lost each time the cell divides.

A

End replication problem

28
Q

A region of repetitive DNA sequences that protect the ends of chromosomes

A

Telomeres

29
Q

As cells divide, the telomere ends of chromosomes get shorter

A

Telomere attrition

30
Q

The limit on cell replication imposed by the shortening of telomeres with each
division.

A

Hayflick limit

31
Q

A reverse transcriptase that adds repeats of a DNA sequence to the ends of
chromosomes.

A

Telomerase

32
Q

There are 2 main models of aging?

A
  1. Damaged-based model
  2. Programmatic models
33
Q

-Conserved methylation sites were highly enriched in polycomb repressive complex 2-binding locations, which
represses the transcription of diverse developmental genes

A

Aging Clocks

34
Q

Methylation clocks indicate aging has a predictable?

A

preset program

35
Q

Age at which RNA expression pattern reverses direction

A

transcriptome Trajectory Turning Points (TTTP):

36
Q
  1. Damaged-based model
A

(Damage to DNA and cells accumulates)

37
Q
  1. Programmatic models
A

(Aging is encoded in the DNA)

38
Q

Peak at ~age 26 =?

A

End of brain development = same time as onset of aging phenotypes

39
Q

Adult cells reprogrammed back into an embryonic-like
pluripotent state that enables them to become any type of cell.

A

induced Pluripotent Stem Cells (iPSC’s)

40
Q

The transcription factors (Oct4 (Pou5f1), Sox2, Klf4 and cMyc) that were used to turn adult cells
into Pluripotent stem cells

A

yamanaka Factors

41
Q
A